Flammable ionic liquids exhibit high conductivity and a broad electrochemical window,enabling the generation of combustible gases for combustion via electrochemical decomposition and thermal decomposition.This charact...Flammable ionic liquids exhibit high conductivity and a broad electrochemical window,enabling the generation of combustible gases for combustion via electrochemical decomposition and thermal decomposition.This characteristic holds significant implications in the realm of novel satellite propulsion.Introducing a fraction of the electrical energy into energetic ionic liquid fuels,the thermal decomposition process is facilitated by reducing the apparent activation energy required,and electrical energy can trigger the electrochemical decomposition of ionic liquids,presenting a promising approach to enhance combustion efficiency and energy release.This study applied an external voltage during the thermal decomposition of 1-ethyl-3-methylimidazole nitrate([EMIm]NO_(3)),revealing the effective alteration of the activation energy of[EMIm]NO_(3).The pyrolysis,electrochemical decomposition,and electron assisted enhancement products were identified through Thermogravimetry-Differential scanning calorimetry-Fourier transform infrared-Mass spectrometry(TG-DSC-FTIR-MS)and gas chromatography(GC)analyses,elucidating the degradation mechanism of[EMIm]NO_(3).Furthermore,an external voltage was introduced during the combustion of[EMIm]NO_(3),demonstrating the impact of voltage on the combustion process.展开更多
ZnO nanosheets doped with yttrium（Y） were synthesized via a solution combustion method using zinc nitrate and tartaric acid as raw materials.The scanning electron microscopy and X-ray powder diffraction were used to...ZnO nanosheets doped with yttrium（Y） were synthesized via a solution combustion method using zinc nitrate and tartaric acid as raw materials.The scanning electron microscopy and X-ray powder diffraction were used to characterize ZnO nanosheets and the gas sensing properties of them were investigated.The results show that the as-synthesized ZnO nanosheets with diameters of20-100 nm have a wurtzite structure with rough surface.The sensor made from the 2%Y-doped ZnO nanosheets exhibits a stronger response toward 100x10-6（volume fraction） ethanol,its sensitivity at 300℃ is 17.50,and its optimal operating temperature（300℃）is lower than that of the pure ZnO（330℃）.The obvious sensitivity（about 2.5） can be observed at the volume fraction of ethanol as low as 5×10-（-6）,while its the response time is only 2s at 300℃.Moreover,the Y-doped ZnO sensor has a better selectivity to ethanol than other gases.展开更多
A different method was employed for the preparation of a metal supported perovskite catalyst for the catalytic combustion of methane.The prepared metallic catalysts were characterized by means of X-ray diffractometer(...A different method was employed for the preparation of a metal supported perovskite catalyst for the catalytic combustion of methane.The prepared metallic catalysts were characterized by means of X-ray diffractometer(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM),and also by ultrasonic and thermal shock tests and catalytic activity.It was found that the process factors during the preparation,e.g.the preparation of the catalyst precursor and the coating slurry,the calcination te...展开更多
Nanocrystal SmBO3 powders were synthesized by nitrate-citrate sol-gel combustion method. The phase evolution, morphologies and absorbency of the synthesized powders were characterized by X-ray diffraction （XRD）, Fie...Nanocrystal SmBO3 powders were synthesized by nitrate-citrate sol-gel combustion method. The phase evolution, morphologies and absorbency of the synthesized powders were characterized by X-ray diffraction （XRD）, Field emission scanning electronic microscope （FESEM）, Fourier transform infrared spectroscopy （FFIR） and UV-3101PC spectrophotometer （UVPC）, respectively. XRD and FESEM results showed that pure SmBO3 phase was obtained at 750 ℃, with an average original particle size of about 100 nm. FTIR showed that there were apparently concentrated absorbent peaks between 500 and 1400 cm^-1. Moreover, the reflectivity of the powders apparently decreased at the wavelength between 1.05 and 1.15 μm. Therefore, SmBO3 might be a kind of absorbent material for infrared laser.展开更多
Cubic and monoclinic Gd2O3:Eu3+ phosphors in the range of nano-scale and submicron-scale were prepared by a modified solution combustion method.Coexistence of cubic and monoclinic phases was found in the highest lumin...Cubic and monoclinic Gd2O3:Eu3+ phosphors in the range of nano-scale and submicron-scale were prepared by a modified solution combustion method.Coexistence of cubic and monoclinic phases was found in the highest luminescent sample synthesized at 600 oC.In relation to commercial sample,the relative luminescence intensity was 49.8%.The shape of emission spectrum of the sample thus changed and the charge-transfer-state band of excitation spectrum slightly shift toward higher energies.With increasing the anneal...展开更多
A 20 wt% Ni/bentonite catalyst was prepared by a solution combustion synthesis (SCS), which exhibited higher activity for the CO_2methanation than that of an impregnation method (IPM), and the catalyst prepared by SCS...A 20 wt% Ni/bentonite catalyst was prepared by a solution combustion synthesis (SCS), which exhibited higher activity for the CO_2methanation than that of an impregnation method (IPM), and the catalyst prepared by SCS showed a CO_2 conversion of 85% and a CH4selectivity of 100% at 300 °C, atmospheric pressure, and 3600 ml·(g cat)-1·h-1, and the catalyst exhibited stable within a 110-h reaction. The results showed higher me- tallic Ni dispersion, smaller Ni particle size, larger specific surface area and lower reduction temperature in the Ni/ bentonite prepared by SCS than that of IPM. And the Ni/bentonite prepared by the SCS moderated the interaction between NiO and bentonite.展开更多
A series of Ceo.sFeo.30Zr0.20O2 catalysts were prepared by different methods （co-precipitations method, citric acid sol-gel method, impregnation method, physical mixed method, and hydrotherrnal method） and character...A series of Ceo.sFeo.30Zr0.20O2 catalysts were prepared by different methods （co-precipitations method, citric acid sol-gel method, impregnation method, physical mixed method, and hydrotherrnal method） and characterized by X-ray diffraction （XRD）, Raman spectroscopy, Brunauer-Emmett-Teller （BET） and H2-TPR measurements. Potential of the catalysts in the soot oxidation was evaluated in a temperature-programmed oxidation （TPO） apparatus. The results showed that all the Fe3＋ and Zr4＋ were incor- porated into ceria lattice to form a pure Ce-Fe-Zr-O solid solution for the co-precipitation sample, but two kinds of Fe phases ex- isted in the Ce-Fe-Zr-O catalysts prepared by other methods： Fe3＋ incorporated into CeO2 lattice and dispersed Fe2O3 clusters. The free Fe2O3 clusters could improve the activity of catalysts for soot oxidation comparing with the pure Ce-Fe-Zr-O solid solution owing to the synergetic effect between free Fe2O3 and surface oxygen vacancies. In addition, the activity of catalysts strongly relied on the surface reducibility of free Fe2O3 particles. Holding both abundant free Fe2O3 particles and high oxygen vacancy concentration, the hydrothermal Ce0.5Fe0.3Zr0.202 catalyst presented the lowest Ti （251℃, ignition temperature of soot oxidation） and Tm （310 ℃, maximum oxidation rate temperature） for soot combustion （with tight-contact between soot and catalysts） among the five samples. Even after aging at 800 ℃ for 10 h, the Ti and Tm were still relatively low, at 273 and 361 ℃, respectively, indicating high catalytic stability.展开更多
Gadolinium zirconate（Gd2Zr2O7） nanocrystals were prepared via two different combustion methods： citric acid combustion（CAC） and stearic acid combustion（SAC）. The effects of the different preparation methods on ...Gadolinium zirconate（Gd2Zr2O7） nanocrystals were prepared via two different combustion methods： citric acid combustion（CAC） and stearic acid combustion（SAC）. The effects of the different preparation methods on the phase composition, microtopography, and sintering densification of the resulting Gd2Zr2O7 nanopowders were investigated by thermal-gravimetric and differential thermal analysis（TG-DTA）, Fourier transform infrared spectroscopy（FTIR）, X-ray diffraction（XRD）, and transmission electron microscopy（TEM） techniques. The results indicated that both methods could produce Gd2Zr2O7 nanopowders with an excellent defective fluorite structure. The reaction time was reduced by the SAC method, compared with the CAC method. The nanopowders synthesized by the two methods were different in grain size distribution. The resulting nanoparticle diameter was about 50 nm for CAC and 10 nm for SAC. After vacuum sintering, the sintered bodies also had a different relative density of about 93% and 98%, respectively. Thus the preparation of Gd2Zr2O7 nanopowders by SAC was the first choice to achieve the desired sintering densification.展开更多
A series of Ni/ZrO_2 catalysts were synthesized by urea combustion method for CO_2 methanation.The effects of zirconium precursors and urea dosage on the structure and catalytic performance of the catalysts were teste...A series of Ni/ZrO_2 catalysts were synthesized by urea combustion method for CO_2 methanation.The effects of zirconium precursors and urea dosage on the structure and catalytic performance of the catalysts were tested.Results showed that the Ni/ZrO_2–O catalyst derived from zirconium oxynitrate hydrate exhibited better catalytic activity than the Ni/ZrO_2 catalyst because of its higher Ni dispersion and smaller Ni particle size.In addition,the urea dosage significantly influenced the low-temperature activity of the catalysts by affecting the metal–support interaction,Ni dispersion,and Ni particle size.The Ni/ZrO_2–O-0.4 catalyst with a urea-to-nitrate molar ratio of 0.4 exhibited the best catalytic activity owing to its moderate metal–support interaction,highest Ni dispersion,and smallest Ni particle size,achieving 69.2% CO_2 conversion and 100% CH_4 selectivity at 300℃,0.1 MPa,and a weight hour space velocity(WHSV)of 50,000 mL/(g·h).Moreover,the urea combustion method can lead to the entire phase transformation from monoclinic ZrO_2 to tetragonal ZrO_2 accompanied by the incorporation of oxygen vacancies in the ZrO_2 lattice.This phenomenon can also be related to the high catalytic activity of the as-prepared catalysts.展开更多
Nanoscale Lu2O3：Eu3＋ phosphor was prepared by a modified solution combustion method using urea and acrylamide monomer.The particle sizes and photoluminescent properties of nano-phosphor were closely related to the m...Nanoscale Lu2O3：Eu3＋ phosphor was prepared by a modified solution combustion method using urea and acrylamide monomer.The particle sizes and photoluminescent properties of nano-phosphor were closely related to the molar ratio of urea-to-RE nitrates and acrylamide monomer-to-RE nitrates.The as-prepared samples with the sizes of 9.6-11.6 nm were characterized by X-ray diffraction,scanning electron microscopy,transmission electron microscopy and energy dispersive spectrometer.Lu2O3：Eu3＋ nano-phosphor that depicted high photoluminescence in the size around 10 nm was reported.Compared with the sample prepared by solid state reaction,the photoluminescence of sample was increased sufficiently to be 45.1%.The emission spectra of the samples presented the typical emission from 5D0 level to 7FJ（J=0,1,2,3,4） level of the Eu3＋ ion.展开更多
AMnO3 （A=Sr, Sm and Nd） manganites with perovskite structure, prepared by combustion method were characterized by X-ray diffraction （XRD）, infra-red spectroscopy, Brunauer-Emmett-Teller （BET） surface area analyz...AMnO3 （A=Sr, Sm and Nd） manganites with perovskite structure, prepared by combustion method were characterized by X-ray diffraction （XRD）, infra-red spectroscopy, Brunauer-Emmett-Teller （BET） surface area analyzer and scanning electron microscopy （SEM）. The solid state and spectroscopic studies such as electrical resistivity, magnetic susceptibility, electron spin resonance （ESR） and diffuse reflectance spectroscopy were carried out and attempted to correlate with the catalytic activities of the compounds. To evaluate the catalytic activity, a model reaction of CO oxidation over these compounds was undertaken. An attempt was made to understand the effect of A-site change by different metal cations in the manganite perovskites on solid state and catalytic properties.展开更多
Titania catalysts were synthesized by a solution combustion method （SCM）. Photodegradation of 4-chlorophenol （4-CP） using the synthesized catalysts was studied under both visible light （λ≥420nm） and sunlight i...Titania catalysts were synthesized by a solution combustion method （SCM）. Photodegradation of 4-chlorophenol （4-CP） using the synthesized catalysts was studied under both visible light （λ≥420nm） and sunlight irradiation. The effect of preparation conditions on photocatalytic activities of the synthesized catalysts was investigated. The optimal photocatalytic activity of the catalyst （denoted as A1 ） was obtained under the following synthesis conditions： ignition temperature of 350~C, fuel ratio （ φ） of 1 and calcination time of lh. The degradation and mineralization ratio of 4-CP were 78.2% and 53.7% respectively under visible light irradiation for 3h using catalyst A1. And the catalyst A1 also showed high photocatalytic activity under sunlight irradiation.展开更多
CaTiO_(3)-LnAlO_(3)(Ln=La,Nd,Sm) is a perovskite-type microwave material system characterized by a moderate dielectric constant εr,a high quality factor Q×f,and a small temperature coefficient of resonant freque...CaTiO_(3)-LnAlO_(3)(Ln=La,Nd,Sm) is a perovskite-type microwave material system characterized by a moderate dielectric constant εr,a high quality factor Q×f,and a small temperature coefficient of resonant frequency τf,making this system promising for microwave devices.However,its high synthesis temperature and sintering temperature limit its industrial applications.In our work,single phase0.7 CaTiO_(3)-0.3 Sm_(0.9)Nd_(0.1)AlO_(3)(7 CT-3 SNA) was synthesized via the sol-gel auto combustion method using citric acid as fuel at a relatively low temperature.After being calcined at 600℃ for 2 h,wellcrystallized 7 CT-3 SNA powders with 30-50 nm average particle size were achieved,suggesting good sintering activity.The new and narrow order band at about 800 cm^(-1) in the Raman spectra indicates a high ordering degree in the B site of 7 CT-3 SNA solid solution.Compared with the solid-state reaction method and co-precipitation method,the 0.7 CT-0.3 SNA ceramics fabricated by the current method possess a much lower calcination temperature,a similar εr value,and an improved Q × f value.The optimum microwave dielectric properties of εr=43.54,Q×f=54375 GHz,and τf=-6.3 ×10^(-6)/℃ are obtained for the CTSA ceramics derived from the sol-gel auto combustion process.Therefore,the 7 CT-3 SNA ceramics prepared in this study are potential dielectric materials for microwave applications,indicating that the sol-gel auto combustion method is a good alternative strategy for the fabrication of CaTiO_(3)-LnAlO_(3) ceramics.展开更多
BaMgAl10Ol7：Eu^2＋,Yb^3＋ was investigated as a possible quantum cutting system to enhance solar cells efficiency. Phosphors were synthesized by combustion method and composed of nanorods. Photoluminescence spectra s...BaMgAl10Ol7：Eu^2＋,Yb^3＋ was investigated as a possible quantum cutting system to enhance solar cells efficiency. Phosphors were synthesized by combustion method and composed of nanorods. Photoluminescence spectra showed that Eu in the sample was reduced to bivalence while Yb remained trivalence. Through a cooperative energy transfer process, the obtained powders exhibited both blue emission of Eu^2＋ （around 450 nm） and near infrared emission of Yb^3＋ （around 1020 nm） under broad band excitation （250-410 nm） originating from 4f→5d transition of Eu2＋. Energy transfer phenomenon between the sensitizer Eu2＋ and the activator Yb3＋ was investigated via the luminescent spectra and the decay curves of Eu2＋ with different Yb3＋ concentrations. Results indicated that energy transfer efficiency from Eu2＋ to Yb3＋ was not high. The poor efficiency can be explained by the long distance between rare earth ions.展开更多
A novel red-emitting phosphor, CaYA1307： Eu^3＋, Sm^3＋, is synthesized by a combustion method at a low temperature （850 ℃）, and the single phase of CaYA1307 is confirmed by powder X-ray diffraction measurements. ...A novel red-emitting phosphor, CaYA1307： Eu^3＋, Sm^3＋, is synthesized by a combustion method at a low temperature （850 ℃）, and the single phase of CaYA1307 is confirmed by powder X-ray diffraction measurements. The photoluminescence property results reveal that the red emission intensity of Eu^3＋ is strongly dependent on the Sm^3＋ concentration. Only the Eu^3＋ luminescence is detected in the Eu^3＋-Sm^3＋ co-doped CaYA1307 phosphor with 393 nm excitation. However, under the characteristic excitation （402 nm） of Sm^3＋, not only the Sm^3＋ emission but also the Eu^3＋ emission are observed. A possible mechanism of the energy transfer between Sm^3＋ and Eu3＋ is investigated in detail.展开更多
Y2O3：Eu3＋ phosphors co-doped with different metal cations （Li＋, Na＋, K＋, Mg2＋, Ca2＋） are prepared by the gel- combustion method with Y2O3：Eu3＋, and R（NO3）x （R = Li, Na, K, Mg, Ca） serving as raw materi...Y2O3：Eu3＋ phosphors co-doped with different metal cations （Li＋, Na＋, K＋, Mg2＋, Ca2＋） are prepared by the gel- combustion method with Y2O3：Eu3＋, and R（NO3）x （R = Li, Na, K, Mg, Ca） serving as raw materials and glycine as fuel, calcined at 1000 ℃ for 2 h. The synthesized Y203 ：Eu3＋ phosphors doped with different metal cations and doping ratios are characterized by x-ray diffractometry （XRD）, fluorescence and phosphorescent spectrophotometer. The co-doping metal cations are advantageous to the development of Y203：Eu3＋ lattice. All the samples can emit red light peaked at 611 nm under 254-nm excited. The luminescence intensities of co-doping samples are increased because the cations increase the electron transition probability of Eu3＋ from 5D0 level to 7F level. The fluorescence lifetime of Eu3＋ （SD0 --＋7F2） is increased by doping metal cations.展开更多
Gadolinium gallium gamet （GGG） nanopowders doped with ytterbium ions （Yb：GGG） were synthesized with citric acid as a fuel via gel combustion method. The optimized conditions for preparing yb^3＋：Gd3Ga5O12 nanopo...Gadolinium gallium gamet （GGG） nanopowders doped with ytterbium ions （Yb：GGG） were synthesized with citric acid as a fuel via gel combustion method. The optimized conditions for preparing yb^3＋：Gd3Ga5O12 nanopowders were discussed. The heat behavior, structure and morphology of powders were analyzed with thermal analysis （TG-DTA）, X-ray diffraction （XRD）, infrared spectra OR） and transmission electron microscope （TEM）. TG-DTA analysis revealed that the weight loss of the precursor occured below 800 ℃ and its crystallization temperature was 830.6℃. XRD and IR analysis showed that the precursor converted directly into pure GGG at a relatively lower temperature （900 ℃） without any other intermediate phase. The lattice constant was 1.2377 calculated by extrapolation method. TEM results indicated that the spherical powders showed good dispersity and had a relatively narrow size distribution with average particle size of approximately 40-50 ran, which was favorable for good sinterability of Yb：GGG laser ceramic.展开更多
Heteroatom doping is an efficient approach to regulate the fluorescence properties of carbon dots.Using aminophenylboronic acid as the raw material,a combustion method was developed for the synthesis of boron,nitrogen...Heteroatom doping is an efficient approach to regulate the fluorescence properties of carbon dots.Using aminophenylboronic acid as the raw material,a combustion method was developed for the synthesis of boron,nitrogen-doped carbon dots（B,N-carbon dots）.The B,N-carbon dots emitted green fluorescence and displayed high resistance to both photo bleaching and ionic strength.A facile fluorescence sensing approach for Cu^2＋ was fabricated via static fluorescence quenching.Under optimal conditions,a rapid detection of Cu^2＋ could be completed in 2 min with a linearity ranging from 1 μmol/L to 25 μmol/L and a detection limit of 0.3 μmol/L Furthermore,the proposed method showed potential applications for the detection of Cu^2＋ in natural water samples.展开更多
GB/T 13245-91 1 Theme and Scope This standard specifies the method abstract, reagents, apparatus, specimen, analyzing procedure, result calculation and permissible tolerance used for determination of the total carbon ...GB/T 13245-91 1 Theme and Scope This standard specifies the method abstract, reagents, apparatus, specimen, analyzing procedure, result calculation and permissible tolerance used for determination of the total carbon with combustion gravimetric method.展开更多
基金supported by the National Natural Science Foundation of China(Grant No.52206165)。
文摘Flammable ionic liquids exhibit high conductivity and a broad electrochemical window,enabling the generation of combustible gases for combustion via electrochemical decomposition and thermal decomposition.This characteristic holds significant implications in the realm of novel satellite propulsion.Introducing a fraction of the electrical energy into energetic ionic liquid fuels,the thermal decomposition process is facilitated by reducing the apparent activation energy required,and electrical energy can trigger the electrochemical decomposition of ionic liquids,presenting a promising approach to enhance combustion efficiency and energy release.This study applied an external voltage during the thermal decomposition of 1-ethyl-3-methylimidazole nitrate([EMIm]NO_(3)),revealing the effective alteration of the activation energy of[EMIm]NO_(3).The pyrolysis,electrochemical decomposition,and electron assisted enhancement products were identified through Thermogravimetry-Differential scanning calorimetry-Fourier transform infrared-Mass spectrometry(TG-DSC-FTIR-MS)and gas chromatography(GC)analyses,elucidating the degradation mechanism of[EMIm]NO_(3).Furthermore,an external voltage was introduced during the combustion of[EMIm]NO_(3),demonstrating the impact of voltage on the combustion process.
基金Project(61079010)supported by the National Natural Science Foundation of ChinaProject(3122013P001)supported by the Significant Pre-research Funds of Civil Aviation University of ChinaProject(MHRD20140209)supported by the Science and Technology Innovation Guide Funds of Civil Aviation Administration of China
文摘ZnO nanosheets doped with yttrium（Y） were synthesized via a solution combustion method using zinc nitrate and tartaric acid as raw materials.The scanning electron microscopy and X-ray powder diffraction were used to characterize ZnO nanosheets and the gas sensing properties of them were investigated.The results show that the as-synthesized ZnO nanosheets with diameters of20-100 nm have a wurtzite structure with rough surface.The sensor made from the 2%Y-doped ZnO nanosheets exhibits a stronger response toward 100x10-6（volume fraction） ethanol,its sensitivity at 300℃ is 17.50,and its optimal operating temperature（300℃）is lower than that of the pure ZnO（330℃）.The obvious sensitivity（about 2.5） can be observed at the volume fraction of ethanol as low as 5×10-（-6）,while its the response time is only 2s at 300℃.Moreover,the Y-doped ZnO sensor has a better selectivity to ethanol than other gases.
基金supported by the Ministry of Science and Technology of Beijing (20081D0500500142)
文摘A different method was employed for the preparation of a metal supported perovskite catalyst for the catalytic combustion of methane.The prepared metallic catalysts were characterized by means of X-ray diffractometer(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM),and also by ultrasonic and thermal shock tests and catalytic activity.It was found that the process factors during the preparation,e.g.the preparation of the catalyst precursor and the coating slurry,the calcination te...
基金supported by the 973 Research Project of China (6134502)
文摘Nanocrystal SmBO3 powders were synthesized by nitrate-citrate sol-gel combustion method. The phase evolution, morphologies and absorbency of the synthesized powders were characterized by X-ray diffraction （XRD）, Field emission scanning electronic microscope （FESEM）, Fourier transform infrared spectroscopy （FFIR） and UV-3101PC spectrophotometer （UVPC）, respectively. XRD and FESEM results showed that pure SmBO3 phase was obtained at 750 ℃, with an average original particle size of about 100 nm. FTIR showed that there were apparently concentrated absorbent peaks between 500 and 1400 cm^-1. Moreover, the reflectivity of the powders apparently decreased at the wavelength between 1.05 and 1.15 μm. Therefore, SmBO3 might be a kind of absorbent material for infrared laser.
基金supported by the Ministry of Science and Technology of China (2006CB601104)the Foundation of International Joint Research of Beijing (2007N08)+1 种基金Natural Science Foundation of Jiangxi Province (2009GQC0042)Foundation of Jiangxi Educational Committee (GJJ10153)
文摘Cubic and monoclinic Gd2O3:Eu3+ phosphors in the range of nano-scale and submicron-scale were prepared by a modified solution combustion method.Coexistence of cubic and monoclinic phases was found in the highest luminescent sample synthesized at 600 oC.In relation to commercial sample,the relative luminescence intensity was 49.8%.The shape of emission spectrum of the sample thus changed and the charge-transfer-state band of excitation spectrum slightly shift toward higher energies.With increasing the anneal...
基金Supported by the National Natural Science Foundation of China(21566005)the Natural Science Foundation of Guangxi Province(2016GXNSFFA380015)
文摘A 20 wt% Ni/bentonite catalyst was prepared by a solution combustion synthesis (SCS), which exhibited higher activity for the CO_2methanation than that of an impregnation method (IPM), and the catalyst prepared by SCS showed a CO_2 conversion of 85% and a CH4selectivity of 100% at 300 °C, atmospheric pressure, and 3600 ml·(g cat)-1·h-1, and the catalyst exhibited stable within a 110-h reaction. The results showed higher me- tallic Ni dispersion, smaller Ni particle size, larger specific surface area and lower reduction temperature in the Ni/ bentonite prepared by SCS than that of IPM. And the Ni/bentonite prepared by the SCS moderated the interaction between NiO and bentonite.
基金Project supported by National Natural Science Foundation of China(51374004,51204083,51174105,51104074)Natural Science Foundation of Yunnan Province(2010ZC018)
文摘A series of Ceo.sFeo.30Zr0.20O2 catalysts were prepared by different methods （co-precipitations method, citric acid sol-gel method, impregnation method, physical mixed method, and hydrotherrnal method） and characterized by X-ray diffraction （XRD）, Raman spectroscopy, Brunauer-Emmett-Teller （BET） and H2-TPR measurements. Potential of the catalysts in the soot oxidation was evaluated in a temperature-programmed oxidation （TPO） apparatus. The results showed that all the Fe3＋ and Zr4＋ were incor- porated into ceria lattice to form a pure Ce-Fe-Zr-O solid solution for the co-precipitation sample, but two kinds of Fe phases ex- isted in the Ce-Fe-Zr-O catalysts prepared by other methods： Fe3＋ incorporated into CeO2 lattice and dispersed Fe2O3 clusters. The free Fe2O3 clusters could improve the activity of catalysts for soot oxidation comparing with the pure Ce-Fe-Zr-O solid solution owing to the synergetic effect between free Fe2O3 and surface oxygen vacancies. In addition, the activity of catalysts strongly relied on the surface reducibility of free Fe2O3 particles. Holding both abundant free Fe2O3 particles and high oxygen vacancy concentration, the hydrothermal Ce0.5Fe0.3Zr0.202 catalyst presented the lowest Ti （251℃, ignition temperature of soot oxidation） and Tm （310 ℃, maximum oxidation rate temperature） for soot combustion （with tight-contact between soot and catalysts） among the five samples. Even after aging at 800 ℃ for 10 h, the Ti and Tm were still relatively low, at 273 and 361 ℃, respectively, indicating high catalytic stability.
文摘Gadolinium zirconate（Gd2Zr2O7） nanocrystals were prepared via two different combustion methods： citric acid combustion（CAC） and stearic acid combustion（SAC）. The effects of the different preparation methods on the phase composition, microtopography, and sintering densification of the resulting Gd2Zr2O7 nanopowders were investigated by thermal-gravimetric and differential thermal analysis（TG-DTA）, Fourier transform infrared spectroscopy（FTIR）, X-ray diffraction（XRD）, and transmission electron microscopy（TEM） techniques. The results indicated that both methods could produce Gd2Zr2O7 nanopowders with an excellent defective fluorite structure. The reaction time was reduced by the SAC method, compared with the CAC method. The nanopowders synthesized by the two methods were different in grain size distribution. The resulting nanoparticle diameter was about 50 nm for CAC and 10 nm for SAC. After vacuum sintering, the sintered bodies also had a different relative density of about 93% and 98%, respectively. Thus the preparation of Gd2Zr2O7 nanopowders by SAC was the first choice to achieve the desired sintering densification.
文摘A series of Ni/ZrO_2 catalysts were synthesized by urea combustion method for CO_2 methanation.The effects of zirconium precursors and urea dosage on the structure and catalytic performance of the catalysts were tested.Results showed that the Ni/ZrO_2–O catalyst derived from zirconium oxynitrate hydrate exhibited better catalytic activity than the Ni/ZrO_2 catalyst because of its higher Ni dispersion and smaller Ni particle size.In addition,the urea dosage significantly influenced the low-temperature activity of the catalysts by affecting the metal–support interaction,Ni dispersion,and Ni particle size.The Ni/ZrO_2–O-0.4 catalyst with a urea-to-nitrate molar ratio of 0.4 exhibited the best catalytic activity owing to its moderate metal–support interaction,highest Ni dispersion,and smallest Ni particle size,achieving 69.2% CO_2 conversion and 100% CH_4 selectivity at 300℃,0.1 MPa,and a weight hour space velocity(WHSV)of 50,000 mL/(g·h).Moreover,the urea combustion method can lead to the entire phase transformation from monoclinic ZrO_2 to tetragonal ZrO_2 accompanied by the incorporation of oxygen vacancies in the ZrO_2 lattice.This phenomenon can also be related to the high catalytic activity of the as-prepared catalysts.
基金Project supported by the Special Foundation for Technique Development Research of Institute of Ministry of Science and Technology of China (2009EG115070,2010EG115072)Natural Science Foundation of Jiangxi Province (2009GQC0042)+1 种基金Foundation of Jiangxi Educational Committee (GJJ10153)Foundation of Jiangxi University of Science and Technology (Jxxjzd10007)
文摘Nanoscale Lu2O3：Eu3＋ phosphor was prepared by a modified solution combustion method using urea and acrylamide monomer.The particle sizes and photoluminescent properties of nano-phosphor were closely related to the molar ratio of urea-to-RE nitrates and acrylamide monomer-to-RE nitrates.The as-prepared samples with the sizes of 9.6-11.6 nm were characterized by X-ray diffraction,scanning electron microscopy,transmission electron microscopy and energy dispersive spectrometer.Lu2O3：Eu3＋ nano-phosphor that depicted high photoluminescence in the size around 10 nm was reported.Compared with the sample prepared by solid state reaction,the photoluminescence of sample was increased sufficiently to be 45.1%.The emission spectra of the samples presented the typical emission from 5D0 level to 7FJ（J=0,1,2,3,4） level of the Eu3＋ ion.
基金supported by UGC,New Delhi,under UGC-SAP program
文摘AMnO3 （A=Sr, Sm and Nd） manganites with perovskite structure, prepared by combustion method were characterized by X-ray diffraction （XRD）, infra-red spectroscopy, Brunauer-Emmett-Teller （BET） surface area analyzer and scanning electron microscopy （SEM）. The solid state and spectroscopic studies such as electrical resistivity, magnetic susceptibility, electron spin resonance （ESR） and diffuse reflectance spectroscopy were carried out and attempted to correlate with the catalytic activities of the compounds. To evaluate the catalytic activity, a model reaction of CO oxidation over these compounds was undertaken. An attempt was made to understand the effect of A-site change by different metal cations in the manganite perovskites on solid state and catalytic properties.
基金Supported by the Key Laboratory of Material-Oriented Chemical Engineering of Jiangsu Province and Ministry of Education.
文摘Titania catalysts were synthesized by a solution combustion method （SCM）. Photodegradation of 4-chlorophenol （4-CP） using the synthesized catalysts was studied under both visible light （λ≥420nm） and sunlight irradiation. The effect of preparation conditions on photocatalytic activities of the synthesized catalysts was investigated. The optimal photocatalytic activity of the catalyst （denoted as A1 ） was obtained under the following synthesis conditions： ignition temperature of 350~C, fuel ratio （ φ） of 1 and calcination time of lh. The degradation and mineralization ratio of 4-CP were 78.2% and 53.7% respectively under visible light irradiation for 3h using catalyst A1. And the catalyst A1 also showed high photocatalytic activity under sunlight irradiation.
基金Project supported by the Natural Science Foundation of Anhui Provincial Education Department (KJ2019A0054)the Student Research and Training Program of Anhui University of Technology (2020008)。
文摘CaTiO_(3)-LnAlO_(3)(Ln=La,Nd,Sm) is a perovskite-type microwave material system characterized by a moderate dielectric constant εr,a high quality factor Q×f,and a small temperature coefficient of resonant frequency τf,making this system promising for microwave devices.However,its high synthesis temperature and sintering temperature limit its industrial applications.In our work,single phase0.7 CaTiO_(3)-0.3 Sm_(0.9)Nd_(0.1)AlO_(3)(7 CT-3 SNA) was synthesized via the sol-gel auto combustion method using citric acid as fuel at a relatively low temperature.After being calcined at 600℃ for 2 h,wellcrystallized 7 CT-3 SNA powders with 30-50 nm average particle size were achieved,suggesting good sintering activity.The new and narrow order band at about 800 cm^(-1) in the Raman spectra indicates a high ordering degree in the B site of 7 CT-3 SNA solid solution.Compared with the solid-state reaction method and co-precipitation method,the 0.7 CT-0.3 SNA ceramics fabricated by the current method possess a much lower calcination temperature,a similar εr value,and an improved Q × f value.The optimum microwave dielectric properties of εr=43.54,Q×f=54375 GHz,and τf=-6.3 ×10^(-6)/℃ are obtained for the CTSA ceramics derived from the sol-gel auto combustion process.Therefore,the 7 CT-3 SNA ceramics prepared in this study are potential dielectric materials for microwave applications,indicating that the sol-gel auto combustion method is a good alternative strategy for the fabrication of CaTiO_(3)-LnAlO_(3) ceramics.
基金Project supported by National Natural Science Foundation of China (11074245, 11074315, 11204292, 11174005)the Fundamental Research Funds for the Central Universities (2340000034)the Funding of Creative Youth by University of Science &Technology of China
文摘BaMgAl10Ol7：Eu^2＋,Yb^3＋ was investigated as a possible quantum cutting system to enhance solar cells efficiency. Phosphors were synthesized by combustion method and composed of nanorods. Photoluminescence spectra showed that Eu in the sample was reduced to bivalence while Yb remained trivalence. Through a cooperative energy transfer process, the obtained powders exhibited both blue emission of Eu^2＋ （around 450 nm） and near infrared emission of Yb^3＋ （around 1020 nm） under broad band excitation （250-410 nm） originating from 4f→5d transition of Eu2＋. Energy transfer phenomenon between the sensitizer Eu2＋ and the activator Yb3＋ was investigated via the luminescent spectra and the decay curves of Eu2＋ with different Yb3＋ concentrations. Results indicated that energy transfer efficiency from Eu2＋ to Yb3＋ was not high. The poor efficiency can be explained by the long distance between rare earth ions.
基金supported by the National Natural Science Foundation of China (Grant Nos. 11204113, 61265004, and 51272097)the Foundation of Application Research of Yunnan Province, China (Grant No. 2011FB022)+2 种基金the Chinese Specialized Research Fund for the Doctoral Program of Higher Education (Grant No. 20115314120001)the Postdoctoral Science Foundation of China (Grant No. 2011M501424)the National Basic Research Program of China (Grant No. 2011CB211708)
文摘A novel red-emitting phosphor, CaYA1307： Eu^3＋, Sm^3＋, is synthesized by a combustion method at a low temperature （850 ℃）, and the single phase of CaYA1307 is confirmed by powder X-ray diffraction measurements. The photoluminescence property results reveal that the red emission intensity of Eu^3＋ is strongly dependent on the Sm^3＋ concentration. Only the Eu^3＋ luminescence is detected in the Eu^3＋-Sm^3＋ co-doped CaYA1307 phosphor with 393 nm excitation. However, under the characteristic excitation （402 nm） of Sm^3＋, not only the Sm^3＋ emission but also the Eu^3＋ emission are observed. A possible mechanism of the energy transfer between Sm^3＋ and Eu3＋ is investigated in detail.
文摘Y2O3：Eu3＋ phosphors co-doped with different metal cations （Li＋, Na＋, K＋, Mg2＋, Ca2＋） are prepared by the gel- combustion method with Y2O3：Eu3＋, and R（NO3）x （R = Li, Na, K, Mg, Ca） serving as raw materials and glycine as fuel, calcined at 1000 ℃ for 2 h. The synthesized Y203 ：Eu3＋ phosphors doped with different metal cations and doping ratios are characterized by x-ray diffractometry （XRD）, fluorescence and phosphorescent spectrophotometer. The co-doping metal cations are advantageous to the development of Y203：Eu3＋ lattice. All the samples can emit red light peaked at 611 nm under 254-nm excited. The luminescence intensities of co-doping samples are increased because the cations increase the electron transition probability of Eu3＋ from 5D0 level to 7F level. The fluorescence lifetime of Eu3＋ （SD0 --＋7F2） is increased by doping metal cations.
基金supported by the Foundation of Ordnance Science Institute (42001070403)
文摘Gadolinium gallium gamet （GGG） nanopowders doped with ytterbium ions （Yb：GGG） were synthesized with citric acid as a fuel via gel combustion method. The optimized conditions for preparing yb^3＋：Gd3Ga5O12 nanopowders were discussed. The heat behavior, structure and morphology of powders were analyzed with thermal analysis （TG-DTA）, X-ray diffraction （XRD）, infrared spectra OR） and transmission electron microscope （TEM）. TG-DTA analysis revealed that the weight loss of the precursor occured below 800 ℃ and its crystallization temperature was 830.6℃. XRD and IR analysis showed that the precursor converted directly into pure GGG at a relatively lower temperature （900 ℃） without any other intermediate phase. The lattice constant was 1.2377 calculated by extrapolation method. TEM results indicated that the spherical powders showed good dispersity and had a relatively narrow size distribution with average particle size of approximately 40-50 ran, which was favorable for good sinterability of Yb：GGG laser ceramic.
基金financially supported by the National Natural Science Foundation of China(No.21375112)the Marine hightech industry development projects of Fujian Province(No.2015-19)
文摘Heteroatom doping is an efficient approach to regulate the fluorescence properties of carbon dots.Using aminophenylboronic acid as the raw material,a combustion method was developed for the synthesis of boron,nitrogen-doped carbon dots（B,N-carbon dots）.The B,N-carbon dots emitted green fluorescence and displayed high resistance to both photo bleaching and ionic strength.A facile fluorescence sensing approach for Cu^2＋ was fabricated via static fluorescence quenching.Under optimal conditions,a rapid detection of Cu^2＋ could be completed in 2 min with a linearity ranging from 1 μmol/L to 25 μmol/L and a detection limit of 0.3 μmol/L Furthermore,the proposed method showed potential applications for the detection of Cu^2＋ in natural water samples.
文摘GB/T 13245-91 1 Theme and Scope This standard specifies the method abstract, reagents, apparatus, specimen, analyzing procedure, result calculation and permissible tolerance used for determination of the total carbon with combustion gravimetric method.
